Department of Chemistry, School of advanced sciences, Vellore Institute of Technology Vellore-632014, Tamilnadu, India.
Department Stem Cells and Regenerative Medicine Centre, Institution Yenepoya Research Centre, Yenepoya University, University Road, Derlakatte, Mangalore 575018, Karnataka, India.
Inorg Chem. 2020 Dec 7;59(23):17689-17711. doi: 10.1021/acs.inorgchem.0c02928. Epub 2020 Nov 19.
Due to several negative issues, market available drugs have been gradually losing their importance in the treatment of cancer. With a view to discover suitable drugs capable of diagnosing as well as inhibiting the growth of cancer cells, we have aspired to develop a group of theranostic metal complexes which will be (i) target specific, (ii) cytoselective, thus rendering the normal cell unaffected, (iii) water-soluble, (iv) cancer cell permeable, and (v) luminescent, being beneficial for healing the cancer eternally. Therefore, to reach our goal, we have prepared novel Ru(II)- and Ir(III)-based bimetallic and hetero bimetallic scaffolds using click-derived pyridinyltriazolylmethylquinoxaline ligands followed by metal coordination. Most of the compounds have displayed significant cytoselectivity against colorectal adenocarcinoma (Caco-2) and epithiloid cervical carcinoma (HeLa) cells with respect to normal human embryonic kidney cells (HEK-293) compared to cisplatin [-diamminedichloroplatinum(II)] along with excellent binding efficacy with DNA as well as serum albumin. Complex (η--cymene)(η-Cp*)RuIrCl(K-N,N-L) [] exhibited the best cytoselectivity against all the human cancer cells and was identified as the most significant cancer theranostic agent in terms of potency, selectivity, and fluorescence quantum yield. Investigation of the localization of complex [] and [] in the more aggressive colorectal adenocarcinoma cell HT-29 indicates that mitochondria are the key cellular target for destroying cancer cells. Mitochondrial dysfunction and G2/M phase cell cycle arrest in HT-29 cell were found to be involved in the apoptotic cell death pathway induced by the test complexes [] and []. These results validate the concept that these types of complexes will be reasonably able to exert great potential for tumor diagnosis as well as therapy in the near future.
由于存在一些负面问题,市售药物在癌症治疗中的重要性逐渐降低。为了发现能够诊断和抑制癌细胞生长的合适药物,我们一直致力于开发一组治疗诊断金属配合物,这些配合物将具有以下特点:(i)靶向特异性,(ii)细胞选择性,从而使正常细胞不受影响,(iii)水溶性,(iv)癌细胞通透性,以及(v)发光性,有利于永久性治愈癌症。因此,为了达到我们的目标,我们使用点击衍生的吡啶基三唑基甲基喹喔啉配体制备了新型 Ru(II)-和 Ir(III)-基双金属和杂双金属支架,然后进行了金属配位。与顺铂[-二氨二氯合铂(II)]相比,大多数化合物对结直肠腺癌(Caco-2)和上皮样宫颈癌(HeLa)细胞具有显著的细胞选择性,而对正常人类胚胎肾细胞(HEK-293)则没有,并且与 DNA 以及血清白蛋白具有良好的结合效力。配合物 (η--cymene)(η-Cp*)RuIrCl(K-N,N-L) []对所有人类癌细胞均表现出最佳的细胞选择性,并且在效力、选择性和荧光量子产率方面被鉴定为最有效的癌症治疗诊断剂。研究配合物 []和[]在侵袭性更强的结直肠腺癌 HT-29 细胞中的定位表明,线粒体是破坏癌细胞的关键细胞靶标。研究发现,HT-29 细胞中线粒体功能障碍和 G2/M 期细胞周期阻滞与测试配合物 []和[]诱导的细胞凋亡途径有关。这些结果验证了这样一种概念,即这些类型的配合物在不久的将来将能够合理地发挥巨大的肿瘤诊断和治疗潜力。